Formulations containing a somatostatin receptor agonist

    公开(公告)号:US11564968B2

    公开(公告)日:2023-01-31

    申请号:US17491837

    申请日:2021-10-01

    申请人: CAMURUS AB

    摘要: The present invention relates to pre-formulations comprising: a) at least one di-acyl lipid; b) at least one phospholipid; c) at least one biocompatible, organic solvent; d) an alkyl ammonium EDTA salt; and e) at least one somatostatin receptor agonist; wherein the pre-formulation has a water content in the range of 0 to 1.0 wt %. The invention further relates to methods of treatment comprising administration of such pre-formulations, to pre-filled administration devices and kits containing the formulations, to the use of an alkylammonium EDTA salt to reduce the decomposition of the lipid components and/or any active agent contained within the pre-formulation.

    CONTROLLED RELEASE PEPTIDE FORMULATIONS

    公开(公告)号:US20210308226A1

    公开(公告)日:2021-10-07

    申请号:US17350363

    申请日:2021-06-17

    申请人: CAMURUS AB

    摘要: The present invention relates to compositions forming a low viscosity mixture of: a)
    20-80 wt. % of at least one diacyl glycerol and/or a tocopherol; b)
    20-80 wt. % of at least one phosphatidyl choline (PC); c)
    5-20 wt. % of at least one biocompatible, organic mono-alcoholic solvent; d)
    up to 20 wt. % polar solvent e)
    at least one peptide active agent; f)
    optionally at least one antioxidant; wherein the ratio of components a:b is in the range 40:60 to 54:46; wherein the pre-formulation forms, or is capable of forming, at least one liquid crystalline phase structure upon contact with excess aqueous fluid. The invention further relates to methods of treatment comprising administration of such compositions, and to pre-filled administration devices and kits containing the formulations.

    Opioid formulations
    4.
    发明授权

    公开(公告)号:US09937164B2

    公开(公告)日:2018-04-10

    申请号:US14416421

    申请日:2013-07-26

    申请人: CAMURUS AB

    IPC分类号: A61K31/4748 A61K31/485

    CPC分类号: A61K31/4748 A61K31/485

    摘要: A depot precursor formulation comprising: a) a controlled-release matrix; b) at least oxygen containing organic solvent; c) at least 12% by weigh of at least one active agent selected from buprenorphine and salts thereof, calculated as buprenorphine free base. Corresponding depot compositions and methods of treatment in pain management, by opioid maintenance and related methods are provided.

    PROSTACYCLIN ANALOGUE FORMULATIONS

    公开(公告)号:US20220387445A1

    公开(公告)日:2022-12-08

    申请号:US17836120

    申请日:2022-06-09

    申请人: CAMURUS AB

    摘要: The present invention relates to an injectable pre-formulation comprising: a) at least one of a mono-, di- or tri-acyl lipid and/or a tocopherol; b) optionally at least one phospholipid; c) at least one biocompatible, organic solvent; and d) at least one prostacyclin analogue or a salt thereof; wherein the pre-formulation forms, or is capable of forming, at least one liquid crystalline phase structure upon contact with excess aqueous fluid. Such compositions may additionally comprise polar co-solvents. Methods of treatment, particularly for management of pulmonary artery hypertension (PAH), severe PAH, Raynaud's disease, ischemia and related conditions are provided, as well as corresponding uses of the compositions. Administration devices comprising the formulations and kits comprising the devices are also provided.

    Prostacyclin analogue formulations

    公开(公告)号:US11369617B2

    公开(公告)日:2022-06-28

    申请号:US16333448

    申请日:2017-09-15

    申请人: CAMURUS AB

    摘要: The present invention relates to an injectable pre-formulation comprising: a) at least one of a mono-, di-, or tri-acyl lipid and/or a tocopherol; b) optionally at least one phospholipid; c) at least one biocompatible, organic solvent; and d) at least one prostacyclin analogue or a salt thereof; wherein the pre-formulation forms, or is capable of forming, at least one liquid crystalline phase structure upon contact with excess aqueous fluid. Such compositions may additionally comprise polar co-solvents. Methods of treatment, particularly for management of pulmonary artery hypertension (PAH), severe PAH, Raynard's disease, ischemia and related conditions are provided, as well as corresponding uses of the compositions. Administration devices comprising the formulations and kits comprising the devices are also provided.

    FORMULATIONS CONTAINING A SOMATOSTATIN RECEPTOR AGONIST

    公开(公告)号:US20220168381A1

    公开(公告)日:2022-06-02

    申请号:US17491837

    申请日:2021-10-01

    申请人: CAMURUS AB

    摘要: The present invention relates to pre-formulations comprising: a) at least one di-acyl lipid; b) at least one phospholipid; c) at least one biocompatible, organic solvent; d) an alkyl ammonium EDTA salt; and e) at least one somatostatin receptor agonist; wherein the pre-formulation has a water content in the range of 0 to 1.0 wt %. The invention further relates to methods of treatment comprising administration of such pre-formulations, to pre-filled administration devices and kits containing the formulations, to the use of an alkylammonium EDTA salt to reduce the decomposition of the lipid components and/or any active agent contained within the pre-formulation.

    INJECTABLE BUPRENORPHINE FORMULATION

    公开(公告)号:US20210308041A1

    公开(公告)日:2021-10-07

    申请号:US17234989

    申请日:2021-04-20

    申请人: CAMURUS AB

    摘要: The present invention provides an injectable liquid formulation comprising: a) a lipid controlled-release matrix comprising at least 50% triacyl lipids; b) at least one oxygen containing organic solvent; c) at least 16% by weight of at least one active agent selected from buprenorphine and salts thereof, calculated as buprenorphine free base. The invention also provides a method for the treatment of pain, for opioid maintenance therapy or for the treatment of opioid dependence by detoxification and/or maintenance or for the treatment or prophylaxis of the symptoms of opioid withdrawal and/or cocaine withdrawal by injecting such a liquid composition.